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Molecular screening for fragile X syndrome in children with unexplained intellectual disability and/or autistic behaviour.
Folia Med (Plovdiv). 2022 Feb 28;64(1):27-32. doi: 10.3897/folmed.64.e60518.
Folia Med (Plovdiv). 2022.
PMID: 35851904
16p11.2 Duplication Syndrome - a Case Report.
Levkova M, Stoyanova M, Staneva R, Hachmeriyan M, Angelova L.
Levkova M, et al. Among authors: hachmeriyan m.
Folia Med (Plovdiv). 2021 Feb 28;63(1):138-141. doi: 10.3897/folmed.63.e52763.
Folia Med (Plovdiv). 2021.
PMID: 33650406
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Comparison between thrombophilic gene polymorphisms among high risk patients.
Levkova M, Hachmeriyan M, Stoyanova M, Miteva V, Angelova L.
Levkova M, et al. Among authors: hachmeriyan m.
Rom J Intern Med. 2020 Mar 1;58(1):20-26. doi: 10.2478/rjim-2019-0021.
Rom J Intern Med. 2020.
PMID: 31469659
Free article.
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Association between polymorphic markers human leucocyte antigen-G and tumour necrosis factor alpha and susceptibility to recurrent miscarriages among Bulgarian women.
Levkova M, Chervenkov T, Hachmeriyan M, Angelova L.
Levkova M, et al. Among authors: hachmeriyan m.
Turk J Obstet Gynecol. 2020 Mar;17(1):34-39. doi: 10.4274/tjod.galenos.2020.48107. Epub 2020 Apr 6.
Turk J Obstet Gynecol. 2020.
PMID: 32341828
Free PMC article.
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CFTR gene variants as a reason for impaired spermatogenesis: a pilot study and a Meta-analysis of published data.
Levkova M, Chervenkov T, Hachmeriyan M, Angelova L.
Levkova M, et al. Among authors: hachmeriyan m.
Hum Fertil (Camb). 2022 Oct;25(4):728-737. doi: 10.1080/14647273.2021.1900608. Epub 2021 Mar 15.
Hum Fertil (Camb). 2022.
PMID: 33719834
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Acute myelogenous leukemia - current recommendations and approaches in molecular-genetic assessment.
Yahya D, Hachmeriyan M, Micheva I, Chervenkov T.
Yahya D, et al. Among authors: hachmeriyan m.
Rom J Intern Med. 2022 Jun 14;60(2):103-114. doi: 10.2478/rjim-2022-0004. Print 2022 Jun 1.
Rom J Intern Med. 2022.
PMID: 35182066
Free article.
Review.
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MLPA in the initial genetic screening of patients with acute myeloid leukemia.
Yahya D, Hachmeriyan M, Ruseva T, Chervenkov T, Micheva I.
Yahya D, et al. Among authors: hachmeriyan m.
Rom J Intern Med. 2024 Mar 23;62(1):44-51. doi: 10.2478/rjim-2023-0027. Print 2024 Mar 1.
Rom J Intern Med. 2024.
PMID: 37948316
Free article.
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A Long-term Follow-up of a Late Diagnosed Patient with Temple Syndrome - a Case Report.
Yordanova N, Iotova V, Mackay DJG, Temple IK, Stoyanova S, Hachmeriyan M.
Yordanova N, et al. Among authors: hachmeriyan m.
J Clin Res Pediatr Endocrinol. 2023 Feb 2. doi: 10.4274/jcrpe.galenos.2022.2022-9-19. Online ahead of print.
J Clin Res Pediatr Endocrinol. 2023.
PMID: 36728278
Free article.
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